Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ilka Klaassen"'
Autor:
Dominique Singer, S Riechardt, Jochen Herrmann, Markus J. Kemper, Monika Wolf, Michael Boettcher, Ilka Klaassen
Publikováno v:
Zeitschrift für Geburtshilfe und Neonatologie. 221:88-91
ZusammenfassungEine 34-jährige 5. Para wurde unserem Zentrum in SSW 36 bei schwerer fetaler Fehlbildung mit Anhydramnion zugewiesen. Die kardiopulmonale Adaptation nach Sectio in SSW 36+1 bei Placentainsuffizienz gestaltete sich weitgehend komplikat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20a3018d829e09c476d8ba2966480c8a
https://doi.org/10.1055/s-0042-111397
https://doi.org/10.1055/s-0042-111397
Autor:
Ilka Klaassen, Bünyamin Özgören, Carolin E. Sadowski, Udo Helmchen, Markus J. Kemper, Jun Oh, Michel Van Husen, Folke Freudenberg, Anja Lehnhardt, Kirsten Timmermann, Kristina Möller
Publikováno v:
Pediatric Nephrology. 30:1477-1483
Steroid-resistant nephrotic syndrome (SRNS) is still regarded as a serious disease although treatment with cyclosporine (CSA) has improved outcome. However, the duration of treatment in responders is unclear, and treatment of patients with genetic ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f09b2df84a94a104fdbc3f4062906a82
https://doi.org/10.1007/s00467-015-3109-3
https://doi.org/10.1007/s00467-015-3109-3
Background. Prognosis of fetuses with renal oligohydramnios (ROH) is often still regarded as poor. Neonatal complications and the long-term follow-up of fetuses with ROH in two pediatric centres are described. Method. 23 fetuses (16 males, 7 females)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66d176506e677fe96134833d22d9e989
http://doc.rero.ch/record/295136/files/gfl591.pdf
http://doc.rero.ch/record/295136/files/gfl591.pdf
Publikováno v:
Zeitschrift für Geburtshilfe und Neonatologie. 217:46-49
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bed7e4e31c6defb02ef1f81f63d48aae
https://doi.org/10.1055/s-0033-1345725
https://doi.org/10.1055/s-0033-1345725
Autor:
Dominique Singer, Georg Hillebrand, Ulrich Budde, Ilka Klaassen, Reinhard Schneppenheim, Wolf A Hassenpflug, Kai Lehmberg, Florian Oyen
Publikováno v:
Zeitschrift fur Geburtshilfe und Neonatologie. 221(1)
We report on 3 male neonates with hereditary ADAMTS13 deficiency (Upshaw Schulman syndrome, USS), the inherited form of thrombotic thrombocytopenic purpura (TTP). 2 presented shortly after birth with thrombocytopenia followed by microangiopathic Coom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c29e0b8ccf9042d4beb4de1825c0bde
https://pubmed.ncbi.nlm.nih.gov/27383044
https://pubmed.ncbi.nlm.nih.gov/27383044
Autor:
Dirk E. Müller-Wiefel, Kristina Möller, Ilka Klaassen, Markus J. Kemper, Lena Herich, Christina Dieterman
Publikováno v:
Pediatric Nephrology. 27:243-249
Adiponectin (ADPN) counteracts the inflammatory response of the endothelium, which plays an important role in the development of atherosclerosis in patients with chronic kidney disease (CKD). Data in children with CKD are scarce. We examined serum AD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e788a18ac4e8a9be54496591a94c54d
https://doi.org/10.1007/s00467-011-1971-1
https://doi.org/10.1007/s00467-011-1971-1
Autor:
Uta Herden, Enke Grabhorn, Florian Brinkert, Markus J. Kemper, Ilka Klaassen, Rainer Ganschow, Bjoern Nashan, Lutz Fischer
Publikováno v:
Transplant International. 24:805-811
Summary In children with renal insufficiency and accompanying or underlying liver disease, combined liver and kidney transplantations (CLKT) are indicated. However, because of the rare indications, the number of paediatric CLKT is low. Our aim was to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e212e5bd417d6232bcdae49883245af
https://doi.org/10.1111/j.1432-2277.2011.01278.x
https://doi.org/10.1111/j.1432-2277.2011.01278.x
Autor:
Konrad Reinshagen, Maja Hempel, Jana Gerling, Michael Boettcher, Stefan Mietzsch, Ilka Klaassen, Dominique Singer, Mareike Pawlik
Publikováno v:
Zeitschrift für Geburtshilfe und Neonatologie. 220:269-270
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa4508c499e0ecc6d57114c0d38c84a0
https://doi.org/10.1055/s-0042-119271
https://doi.org/10.1055/s-0042-119271
Autor:
Anja Lehnhardt, Michael van Husen, Markus J. Kemper, D. E. Müller-Wiefel, Kristina Möller, Ann-Katrin Fischer, Ilka Klaassen
Publikováno v:
Kidney International. 78(2):200-206
Fibroblast growth factor 23 (FGF23) is a circulating protein that regulates the renal reabsorption of phosphate and also inhibits 1-alpha-hydroxylase production. In adults FGF23 is increased in chronic kidney disease (CKD) and is an important prognos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ead7a614f19338dada2d60e50bc5180e
Autor:
Ilka Klaassen
Publikováno v:
Dialyse aktuell. 13:484-492
Congenital renal failure is rare, the major cause are congenital anomalies of the kidney and the urinary tract. The renal impairment can occur in utero presenting oligohydramnios and may cause pulmonary hypoplasia. Outcome for these fetuses is still
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f89daeb1650da1b924c7de85fef9ec43
https://doi.org/10.1055/s-0029-1243596
https://doi.org/10.1055/s-0029-1243596